Carried out under high-vacuum conditions (~5x10-7. Low energy atoms (~0.1 ev) leave little surface damage

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Eaporation Resistie eaporation Uses resistie heating to eaporate a metallic filament Drawbacks Limited to low melting point metals Small filament size limits deposit thickness Electron-beam eaporation Uses a stream of high energy electrons (5-30 kev) to eaporate source material Can eaporate any material Electron-beam guns with power up to 1200 kw Drawbacks At >10k incident electrons can produce x-rays Redeposition of metal droplets blown of source by apor Ion beam eaporation Inductie heating eaporation Physical apor deposition: thermal eaporation high acuum to aoid contamination line-of-sight deposition, poor step coerage heating of source material potential problem: thermal decomposition rates ~ 0.1- few nm/sec typically P apor ~ 10-4 orr immediately aboe source pressure at sample surface is much lower few monolayers per sec «P equi ~ 10-6 orr 10 0 10-1 10-2 10-3 10-4 Dean P. Neikirk 2001, last update February 2, 2001 21 Dept. of ECE, Uni. of exas at Austin Eaporation Material is heated to attain gaseous state Carried out under high-acuum conditions (~5x10-7 torr) Adantages Films can be deposited at high rates (e.g., 0.5 µm/min) Low energy atoms (~0.1 e) leae little surface damage Little residual gas and impurity incorporation due to highacuum conditions No substrate heating Eaporation Limitations Accurately controlled alloy compounds are difficult to achiee No in situ substrate cleaning Poor step coerage Variation of deposit thickness for large/multiple substrates X-ray damage apor pressure (orr) 10-5 Na : melting point Ag In Al Ga i Au Ni i Cr Pt Mo W 10-6 0 500 1000 1500 2000 2500 emperature ( C) adapted from Campbell, p. 284.

Eaporation Support Materials Refractory metals: ungsten (W); MP = 3380 C, P* = 10-2 torr at 3230 C antalum (a); MP = 3000 C, P* = 10-2 torr at 3060 C Molybdenum (Mo); MP = 2620 C, P* = 10-2 torr at 2530 C Refractory ceramics: Graphitic Carbon (C); MP = 3700 C, P* = 10-2 torr at 2600 C Alumina (Al 2 O 3 ); MP = 2030 C, P* = 10-2 torr at 1900 C Boron nitride (BN); MP = 2500 C, P* = 10-2 torr at 1600 C Engineering considerations: hermal conductiity hermal expansion Electrical conductiity Wettability and reactiity Resistance Heated Eaporation Simple, robust, and in widespread use. Can only achiee temperatures of about 1800 C. Use W, a, or Mo filaments to heat eaporation source. ypical filament currents are 200-300 Amperes. Exposes substrates to isible and IR radiation. ypical deposition rates are 1-20 Angstroms/second. Common eaporant materials: Au, Ag, Al, Sn, Cr, Sb, Ge, In, Mg, Ga CdS, PbS, CdSe, NaCl, KCl, AgCl, MgF 2, CaF 2, PbCl 2 hermal eaporation main heating mechanisms resistiely heat boat containing material tungsten (mp 3410Û&WDQWDOXPPSÛ&PRO\EGHQXPPS 2617Û&YHU\FRPPRQ³KHDWHU PDWHULDOV reaction with boat potential problem electron beam electron beam eaporator source material directly heated by electron bombardment can generate x-rays, can damage substrate/deices I beam ~ 100 ma, V acc ~ kv «P ~ kwatts source material hearth Vacc B field hot filament Iheater inductiely heat material (direct for metals) essentially eddy current losses Dean P. Neikirk 2001, last update February 2, 2001 22 Dept. of ECE, Uni. of exas at Austin Eaporation System Requirements Vacuum: Need 10-6 torr for medium quality films. Can be accomplished in UHV down to 10-9 torr. Cooling water: Hearth hickness monitor Bell jar Mechanical shutter: Eaporation rate is set by temperature of source, but this cannot be turned on and off rapidly. A mechanical shutter allows eaporant flux to be rapidly modulated. Electrical power: Either high current or high oltage, typically 1-10 kw.

Electron Beam Heated Eaporation Source 270 degree bent electron beam pyrolytic graphite hearth liner eaporation cones of material magnetic field 4-pocket rotary copper hearth (0 V) recirculating cooling water cathode filament (-10,000 V) beam forming aperture Electron Beam Heated Eaporation - 2 270 bent beam electron gun is most preferred: Filament is out of direct exposure from eaporant flux. Magnetic field can be used for beam focusing. Magnetic field can be used for beam positioning. Additional lateral magnetic field can be used produce X-Y sweep. Sweeping or rastering of the eaporant source is useful for: Allows a larger eaporant surface area for higher deposition rates. Allows initial charge to be soaked or preheated. Allows eaporant source to be more fully utilized. Multiple pocket rotary hearth is also preferred: Allows sequential deposition of layers with a single pump-down. Allows larger eaporation sources to be used. Resistance Heated Eaporation Sources foil dimple boat wire hairpin alumina coated foil dimple boat wire helix foil trough wire basket chromium coated tungsten rod alumina crucible with wire basket alumina crucible in tantalum box Electron Beam Heated Eaporation - 1 More complex, but extremely ersatile. Can achiee temperatures in excess of 3000 C. Use eaporation cones or crucibles in a copper hearth. ypical emission oltage is 8-10 kv. Exposes substrates to secondary electron radiation. X-rays can also be generated by high oltage electron beam. ypical deposition rates are 10-100 Angstroms/second. Common eaporant materials: Eerything a resistance heated eaporator will accommodate, plus: Ni, Pt, Ir, Rh, i, V, Zr, W, a, Mo Al 2 O 3, SiO, SiO 2, SnO 2, io 2, ZrO 2

Condensation of Eaporant - 1 Condensation of a apor to a solid or liquid occurs when the partial pressure of the apor exceeds the equilibrium apor pressure of the condensed phase at this temperature. he apor is supersaturated under these conditions. his is only true if condensation takes place onto material which is of the same composition as the apor. When a material is first deposited onto a substrate of a different composition, a third adsorbed phase must be included to describe the process. Condensation of Eaporant - 2 Molecules impinging upon a surface may: Adsorb and permanently stick where they land (rare!). Adsorb and permanently stick after diffusing around on the surface to find an appropriate site. his can lead to physisorption or chemisorption. Adsorb and then desorb after some residence time τ a. Immediately reflect off of the surface. Incident apor molecules normally hae a kinetic energy much higher than k B of the substrate surface. Whether an atom or molecule will stick depends upon how well it can equilibrate with the substrate surface, decreasing its energy to the point where it will not subsequently desorb. High hroughput Eaporation echniques Box coaters are used for eaporating large substrate materials, often up to seeral meters in size. Large amounts of source material are required, but cannot be all heated at once because of realistic power limitations. wo popular techniques: Powder trickler source Wire feed source Both can be adapted for either resistance heated or electron beam heated eaporation systems. Adsorption Adsorption is the sticking of a particle to a surface. Physisorption: he impinging molecule loses kinetic (thermal) energy within some residence time, and the lower energy of the molecule does not allow it to oercome the threshold that is needed to escape. Chemisorption: he impinging molecule loses its kinetic energy to a chemical reaction which forms a chemical bond between it and other substrate atoms.

Condensation of Eaporant - 5 If the impingement rate stops, then the adsorbed molecules will all eentually desorb. Condensation of a permanent deposit will not occur, een for low substrate temperatures, unless the molecules interact. Within the mean residence time, surface migration occurs and clusters form. Clusters hae smaller surface-to-olume ratios, and therefore desorb at a reduced rate. Nucleation of a permanent deposit is therefore dependent upon clustering of the adsorbed molecules. Obsered Growth of a Deposited Film Adsorbed monomers Subcritical embryos of arious sizes Formation of critically sized nuclei Growth of nuclei to supercritical size and depletion of monomers within their capture zones Nucleation of critical clusters within non-depleted areas Clusters touch and coalesce into new islands, exposing fresh substrate areas Adsorption of monomers onto fresh areas Larger islands grow together leaing holes and channels Channels and holes fill to form a continuous film Condensation of Eaporant - 3 hermal accomodation coefficient: E E r α = = E E E, = energy, temperature of impinging apor molecules. E r, r = energy, temperature of resident apor molecules; (hose which hae adsorbed, but hae not permanently found a site.) E s, s = energy, temperature of substrate surface. If α < 1, (E r > E s ), then some fraction of the impinging molecules will desorb from the surface. s r s Condensation of Eaporant - 4 Mean residence time for an adsorbed molecule: 1 G des τ = a υ exp 0 k B υ 0 = k B /h = ibrational frequency of adsorbed molecule (~10 14 Hz) his is the frequency at which the molecule attempts to desorb. G des = free actiation energy for desorption. Under a constant impinging apor flux of R, the surface density of the deposit is then: n s = R τ a R = deposition rate in molecules/cm 2 -sec. n s = surface density of deposited molecules in cm -2. = R υ exp 0 k G B des

Sputtering Sputtering Limitations Deposition rate of some materials quite low Some materials (e.g., organics) degrade due to ionic bombardment Incorporation of impurities due to low-medium acuum Condensation Control Control of condensation of the eaporant is achieed through the control of substrate temperature s. Higher substrate temperatures: Increase thermal energy of adsorbed molecules. (Shortens the residence time.) Increase surface diffusiity of adsorbed molecules. Performs annealing of deposited film. Substrate heaters: Quartz IR lamps from frontside a, W, or Mo foil heaters from backside Graphite impregnated cloth heaters from backside oo much heat will desorb the deposited film, eaporating it away! (But this can be used for cleaning ) Sputtering Uses high energy particles (plasma) to dislodge atoms from source surface Carried out under low-medium acuum (~10 mtorr) Adantages Can use large area targets for uniform thickness oer large substrates Easy film thickness control ia time Ease of alloy deposition Substrate surface can be sputter cleaned (etched) Step coerage Sufficient material for many depositions No x-ray damage

Sputtering use moderate energy ion bombardment to eject atoms from target purely physical process can deposit almost anything 3 2 1 sputtering yield (ejected atoms / incident ion) 0 Au i Si 200 400 600 800 1000 Ion energy (ev) Pt Al Cr W adapted from: Campbell, p. 295 Dean P. Neikirk 2001, last update February 2, 2001 23 Dept. of ECE, Uni. of exas at Austin Sputtering plasma generates high density, energetic incident particles magnetic field used to confine plasma, electric field ( bias ) to accelerate dc plasma: metals rates up to ~1 µm / minute rf plasma: dielectrics typically inert (noble) gas used to form incident ions ion energies ~ few hundred ev ; ejected atoms ~ tens ev ~10-2 orr, λ ~ 5 mm better step coerage than eaporation B field E field plasma plasma B field target E field planar magnetron target S-gun conical magnetron adapted from: Campbell, p. 298 Dean P. Neikirk 2001, last update February 2, 2001 24 Dept. of ECE, Uni. of exas at Austin